{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-04-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Dieren",
      "state": "",
      "country": "Netherlands",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83607",
      "recalling_firm": "Vital Scientific N.V.",
      "address_1": "24, Kanaalweg",
      "address_2": "Postbus 100",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "US in the state of New York.",
      "recall_number": "Z-2558-2019",
      "product_description": "V-Twin, Model # 6002-800, UDI: 03661540600180    Product Usage:  An in-vitro diagnostic device, which is an automated chemistry analyzer, micro type, intended for clinical use in conjunction with certain materials to measure a variety of analytes, including applications in clinical chemistry, monitoring drugs of abuse and in therapeutic drug monitoring.",
      "product_quantity": "2",
      "reason_for_recall": "Instrument stopped working due to a software lockup, and no patient results are produced.",
      "recall_initiation_date": "20160118",
      "center_classification_date": "20190923",
      "report_date": "20191002",
      "code_info": "Serial #s: 13-3341  and 13-3344",
      "more_code_info": ""
    }
  ]
}